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diethyl α-(phenylsulfonylamino)-3-fluorobenzylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 929049-07-0 Structure
  • Basic information

    1. Product Name: diethyl α-(phenylsulfonylamino)-3-fluorobenzylphosphonate
    2. Synonyms: diethyl α-(phenylsulfonylamino)-3-fluorobenzylphosphonate
    3. CAS NO:929049-07-0
    4. Molecular Formula:
    5. Molecular Weight: 401.396
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 929049-07-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: diethyl α-(phenylsulfonylamino)-3-fluorobenzylphosphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl α-(phenylsulfonylamino)-3-fluorobenzylphosphonate(929049-07-0)
    11. EPA Substance Registry System: diethyl α-(phenylsulfonylamino)-3-fluorobenzylphosphonate(929049-07-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 929049-07-0(Hazardous Substances Data)

929049-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929049-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,0,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 929049-07:
(8*9)+(7*2)+(6*9)+(5*0)+(4*4)+(3*9)+(2*0)+(1*7)=190
190 % 10 = 0
So 929049-07-0 is a valid CAS Registry Number.

929049-07-0Downstream Products

929049-07-0Relevant articles and documents

N-sulfonyl-and N-phosphorylbenzimidoylphosphonates

Kolotilo,Sinitsa,Rassukanaya,Onys'ko

, p. 1210 - 1218 (2006)

A procedure for preparing N-sulfonyl-and N- phosphorylbenzimidoylphosphonates by oxidation of the corresponding α-(sulfonylamino)-and α-(phosphorylamino)benzylphosphonates was developed. The σ constants of imidoylphosphonate groups were evaluated by 19F NMR spectroscopy, and specific features of their electronic effects were considered. The reactions of the imidoylphosphonates obtained with O-, S-, P-, and N-nucleophiles were studied. The phosphonate-phosphoramidate rearrangement of α-aminobenzylidene-bisphosphonates was found. Nauka/Interperiodica 2006.

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